Influence of the chromophore ionization potential on speed and magnitude of photorefractive effects in poly(N-vinylcarbazole) based polymer composites

被引:24
|
作者
Van Steenwinckel, D
Hendrickx, E
Persoons, A
Van den Broeck, K
Samyn, C
机构
[1] Katholieke Univ Leuven, Ctr Res Mol Elect & Photon, Lab Chem & Biol Dynam, B-3001 Louvain, Belgium
[2] Katholieke Univ Leuven, Lab Macromol & Phys Organ Chem, B-3001 Louvain, Belgium
来源
JOURNAL OF CHEMICAL PHYSICS | 2000年 / 112卷 / 24期
关键词
D O I
10.1063/1.481743
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We report on the synthesis of three highly polar chromophores and their use as dopants in poly(N-vinylcarbazole) based photorefractive polymer composites sensitized with (2,4,7-trinitro-9-fluorenylidene)malononitrile. Small alterations in the amino donor group substituents were used to tune the dye's ionization potential (IP) by 0.2 eV. At 780 nm, 5 degrees C above the glass transition temperature (T-g), and with an applied field of 59 V/mu m, we observed complete internal diffraction and a gain coefficient of 167 cm(-1). In this temperature range, diffraction efficiency, gain coefficient, and photorefractive phase shift were found to correlate with the chromophore IP. At 20 degrees C below Tg, the contribution from birefringence to the index modulation is insignificant, and the speed of the photorefractive effect correlates well with the chromophore IP. Analysis of the results suggests that the space-charge field is influenced by the chromophore IP. (C) 2000 American Institute of Physics. [S0021-9606(00)70224-8].
引用
收藏
页码:11030 / 11037
页数:8
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